Remote Senior Regulatory Writing & Medical Affairs Manager

eTeam; Raynham (MA); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading medical device company is seeking a Medical Writer Specialist to prepare regulatory documents and conduct scientific writing. This role demands a Ph.D/Pharm D or an equivalent degree with 1-2 years of relevant experience, or a BS/B.Pharm/BSN/MS/MPH with 4-5 years. The candidate should have excellent writing skills, knowledge of clinical research, and proficiency in Microsoft Office Suite. The position is based in Raynham, MA, with options for remote work for experienced professionals.

Qualifications

• Ph.D/Pharm D in medical writing or related field.
• 1-5 years of medical device/drug industry experience.
• Expertise in clinical research, regulations, and scientific writing.

Responsibilities

• Prepare, write, edit, and review regulatory documents.
• Conduct literature reviews for post-market activities.
• Perform scientific writing, including abstracts and manuscripts.
• Ensure documents follow internal and external guidelines.
• Communicate with various departments for information.

Skills

Excellent writing and proofreading

Project management

Strong oral communication

Interpersonal skills

Education

Ph.D/Pharm D plus 1-2 years experience or BS/B.Pharm/BSN or MS/MPH plus 4-5 years experience

Tools

Microsoft Office Suite

Bibliographic software (e.g. Endnote, Reference Manager)

Job description

A leading medical device company is seeking a Medical Writer Specialist to prepare regulatory documents and conduct scientific writing. This role demands a Ph.D/Pharm D or an equivalent degree with 1-2 years of relevant experience, or a BS/B.Pharm/BSN/MS/MPH with 4-5 years. The candidate should have excellent writing skills, knowledge of clinical research, and proficiency in Microsoft Office Suite. The position is based in Raynham, MA, with options for remote work for experienced professionals.